Classifications

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  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
  • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
  • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
  • C07D213/16—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom containing only one pyridine ring
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
  • C07C251/02—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups
  • C07C251/20—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups having carbon atoms of imino groups being part of rings other than six-membered aromatic rings
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
  • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/04—Centrally acting analgesics, e.g. opioids
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/20—Hypnotics; Sedatives
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
  • A61P9/06—Antiarrhythmics
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
  • A61P9/08—Vasodilators for multiple indications
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
  • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
  • C07C251/32—Oximes
  • C07C251/50—Oximes having oxygen atoms of oxyimino groups bound to carbon atoms of substituted hydrocarbon radicals
  • C07C251/58—Oximes having oxygen atoms of oxyimino groups bound to carbon atoms of substituted hydrocarbon radicals of hydrocarbon radicals substituted by nitrogen atoms not being part of nitro or nitroso groups
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
  • C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
  • C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
  • C07D295/084—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
  • C07D295/088—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C2601/00—Systems containing only non-condensed rings
  • C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C2601/00—Systems containing only non-condensed rings
  • C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
  • C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C2601/00—Systems containing only non-condensed rings
  • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
  • C07C2601/14—The ring being saturated
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C2601/00—Systems containing only non-condensed rings
  • C07C2601/18—Systems containing only non-condensed rings with a ring being at least seven-membered

Definitions

• the present invention relates to novel, pharmaceutically active, racemic or optically active compounds of formula I ##STR2## wherein R and R 1 are independently hydrogen atom, halogen atom, lower alkoxy, or together represent a methylene dioxy group,
• R 2 and R 3 together represent a chemical bond or independently stand for a hydrogen atom
• R 4 and R 5 are independently hydrogen atom, C 3-7 cycloalkyl group or straight or branched, saturated or unsaturated C 1-12 alkyl group optionally substituted by one or more dialkyl-aminoalkyl, dimethoxyphenyl or phenyl groups, or
• R 4 and R 5 together with the adjacent nitrogen atom form a 4 to 7 membered ring optionally comprising an oxygen, sulfur or a further nitrogen atom, which ring is optionally substituted by a phenyl, benzyl or C 1-3 alkyl group and the said substituents may carry a hydroxy group, one or two methoxy groups, halogen atoms or trifluoromethyl groups, or
• R 4 and R 5 together with the adjacent nitrogen atom form a piperidine ring which is optionally substituted by a phenyl or benzyl group and, if desired, it comprises a double bond,
• R 6 stands for hydrogen atom or benzoyl group
• n an integer from 3 to 6, the acid-addition salts and quaternary ammonium derivatives thereof as well as cardiac circulation controlling and/or improving, central nervous system tranquillizing and/or digestive system irregulations improving pharmaceutical compositions containing these compounds.
• the invention also relates to all of the possible stereoisomers of aminopropanol derivatives of formula I and to the mixture thereof.
• the invention also covers the preparation of compounds of formula I.
• the fluorene derivative "IPS-339" of formula (a) ##STR3## exhibits beta-adrenergic blocking effect.
• Peraclopone (compound of formula d) ##STR6## reduces the level of lipids.
• U.S. Pat. No. 4,652,586 relates to compounds of formula IX, wherein L is fluorene and B is a secondary amino group.
• the compounds reduce the inner pressure of eye and exhibit selective beta-two-adrenergic antagonist effect.
• novel aminopropanol derivatives of formula I is basicly different from that of the prior art compounds.
• the activity of the novel compounds of the invention is surprising and non-predictable as though few of the novel aminopropanol derivatives of formula I exhibit antiarrhythmic activity, this activity is not based on beta-adrenergic blocking effect.
• novel aminopropanol derivatives of formula I can be prepared in several manners.
• the novel aminopropanol derivatives of formula I can be prepared by reacting a cycloalkane derivative of formula II, wherein R, R 1 , R 2 , R 3 and n are the same as defined hereinabove and A represents a group of formula ⁇ N--OH, with a halogen derivative of formula III, wherein L is halogen atom and R 7 and R 8 together represent an oxygen atom, and reacting a compound of formula VIII, ##STR11## thus obtained, wherein R, R 1 , R 2 , R 3 and n are the same as defined hereinabove, with an amine of formula V, wherein R 4 and R 5 are the same as defined hereinabove and R 9 represents hydrogen atom.
• the novel aminopropanol derivatives of formula I can be prepared by reacting a compound of formula II, wherein R, R 1 , R 2 , R 3 and n are the same as defined hereinabove and A represents oxygen or sulfur atom, with a glycol derivative of formula III, wherein L represents H 2 N--O-- or the acid-addition salt thereof and R 7 and R 8 are independently hydroxyl groups, and reacting the glycol derivative of formula VI ##STR12## thus obtained, wherein R, R 1 , R 2 , R 3 and n are the same as defined hereinabove, first with thionyl chloride, then with an amine of formula V, wherein R 4 and R 5 are the same as defined hereinabove and R 9 represents hydrogen atom.
• novel aminopropanol derivatives of formula I wherein R 6 represents hydrogen atom, while R, R 1 , R 2 , R 3 , R 4 , R 5 and n are the same as defined hereinabove, can be reacted with a reactive benzoic acid derivative, preferably with benzoic acid anhydride, to obtain novel aminopropanol derivatives of formula I, wherein R, R 1 , R 2 , R 3 , R 4 , R 5 and n are the same as defined hereinabove and R 6 is benzoyl group.
• the temperature of the reaction can vary within wide ranges.
• the reaction can be completed even at room temperature, but according to our experiments the optimal reaction rate can be achieved at the boiling point of the reaction mixture.
• novel aminopropanol derivatives of formula I are prepared by reacting a compound of formula II with a compound of formula III, wherein R, R 1 , R 2 , R 3 and n are the same as defined hereinabove, L is halogen atom, A is a group of formula ⁇ N--OH, while R 7 and R 8 together represent an oxygen atom, and the epoxy compound of formula VIII thus obtained is aminated with a compound of formula V, wherein R 4 and R 5 are the same as defined hereinabove and R 9 is hydrogen atom, then the reaction is carried out in an inert or relatively inert solvent in the presence of a basic condensing agent.
• inert solvent preferably sodium amide or sodium hydride is used.
• an alkali metal amide or hydride is used as solvent.
• the alcohols e.g. ethyl alcohol and propyl alcohols
• water is a suitable solvent.
• water is a "relatively inert solvent" as it reacts with the epoxy ring after a longer reaction time and at higher temperatures.
• the amination of the epoxy compound can be carried out in an inert medium, such as alcohols, e.g.
• novel aminopropanol derivatives of formula I are prepared by reacting a compound of formula II with a compound of formula III, wherein R, R 1 , R 2 , R 3 and n are the same as defined hereinabove, L is H 2 N--O-- and R 7 and R 8 independently represent a hydroxyl group each
• the reaction can be carried out in inert solvents, e.g. in alcohols, such as methyl or ethyl alcohol, benzene and the homologues thereof, ethers, etc. in the presence of an organic base, e.g. pyridine, lutidine, triethyl amine.
• the reaction can also be carried out by using the excess of the organic base as solvent.
• glycol derivatives thus obtained can be reacted with thionyl chloride in an inert solvent, preferably in halogenated paraffins (such as dichloroethane, dichloromethane, chloroform, etc.), and the 1,2,3-dioxathiolane-2-oxide derivative thus obtained can be reacted with an amine of formula V, wherein R 4 and R 5 are the same as defined hereinabove and R 9 is hydrogen atom, in an inert solvent or without solvent.
• halogenated paraffins such as dichloroethane, dichloromethane, chloroform, etc.
• novel aminopropanol derivatives of formula I can be transformed into pharmaceutically acceptable acid-addition salts or quaternary ammonium derivatives.
• acid-addition salts hydrogen halides, sulfuric acid, phosphoric acid, tartaric acid, succinic acid, acetic acid, fumaric acid, maleic acid, methanesulfonic acid, propionic acid, etc. can be used.
• quaternary ammonium compounds the compounds of formula I are reacted with reactants suitable for quaternarization, e.g. with alkyl halides.
• novel aminopropanol derivatives of formula I may comprise one or two asymmetric carbon atoms depending on the character of the substituents, thus one or more racemic or two or more optically active forms of compounds of formula I can be prepared.
• the invention covers all of the racemic and optically active forms of compounds of formula I. If the former compounds or intermediates are prepared in the form of a diastereomeric mixture, then they can be separated into the racemic or optically active isomers in a manner known per se, by e.g. fractionated distillation, crystallization, chromatography or by forming diastereomeric salts with the aid of optically active acids, such as tartaric acid, dibenzoyl tartaric acid or camphorsulfonic acid.
• novel aminopropanol derivatives of formula I proved to be biologically active upon testing for pharmaceutical activity.
• the most significant ones are the antianginal and/or antiarrhythmic activity, inhibition of stomach secretion (gastric acid secretion), local anaesthetic, tranquillo-sedative, antiinflammatory, analgesic and in some cases calcium antagonistic activity.
• the test for acute toxicity was carried out by using 10 white mice (CFLP strain) (both male and female), weighing 18 to 22 g in each dose group.
• the compounds of the invention were administered orally in a dose of 20 ml/kg.
• mice were administered orally with the compounds of the invention, then both the control and the test groups were intravenously added 40 mg/kg of hexobarbital in order to make the mice sleep (Kaergard et al.).
• the test was carried out by using the modified method of Marmo et al. on rats weighing 160 to 200 g.
• the animals were narcotised by ethyl uretane (1.2 g/kg ip.).
• Aconitin was administered intravenously in a dose of 75 ⁇ g/kg in the form of a bolus injection.
• the ECG alterations were monitored in standard II lead by 5 minutes after the administration of aconitine.
• the observed alterations were classified into classes 0 to 5.
• the compounds of the invention were administered 2 minutes or 60 minutes before the parenteral or oral administration of aconitine, respectively.
• class 2 each second one is an extrasystole
• the compound according to Example 1 administered orally has a multiplied effect compared to the control compounds regarding the absolute dose, its therapeutical activity range is 5.8 times higher than that of Quinidine.
• the test was carried out by using rats weighing 180 to 220 g.
• the animals were narcotised by chloralose urethane (70 to 700 mg/kg ip.).
• the ECG alterations were registered in standard II lead with the aid of needle electrodes.
• the antianginal effect was measured with Nieschultz's method.
• the coronary insufficiency was caused by vasopressine (1 NE/kg, iv.).
• the size of the T-wave was measured before and after administration of vasopressine in both the control and test groups.
• the compounds of the invention were administered 2 minutes before the administration of vasopressine. (Nieschulz, O., Popendiker, K., Hoffmann, I.: Arzneistoff-Forschung 5, 680/1955/)
• test material was injected around the nervus ischiadicus in the middle of femur with a needle of 1 cm length.
• the criterion of analgesic effect was the lack of the motoric control of foot muscles.
• the test was carried out according to Shay's operational method. Rats weighing 200 to 250 g were fastened for 48 hours. On the day of the test the pylorus of the animals was bound under ether narcosis. The test compounds were administered orally 3 hours before the operation. The animals of the control group were administered with the carrier only. 4 hours after the operation the stomach was removed, the content thereof was centrifuged and the amount of free acid was determined by titration with 0.1N sodium hydroxide.
• the activity of the compounds of the present invention reach or exceed the activity of Cimetidine and highly exceed the secretion inhibiting effect of Trithiozine. (Shay, H., Komarov, S. A., Fels, S. S., Meranze, D., Gruenstein, M., Siplet, H.: Gastroenterology 5, 45/1945/)
• the antiperistaltic effect of the compounds was examined by the method of Stickney et al. on white mice of both sexes, weighing 20 to 25 g.
• the compounds to be tested were administered per os 60 minutes before the addition of carbon suspension to groups containing 10 mice each.
• the animals of the control groups were treated at the same time and in the same manner with the carrier only.
• the mice were killed 10 minutes after the addition of the carbon suspension, and the whole length of the intestines as well as the length of the intestines filled with carbon suspension were measured.
• the compounds of formula I according to the invention can well be absorbed if administered either orally or parenterally.
• the compound of formula (e) described in U.S. Pat. No. 4,621,101 is known as an excellent antiarrhythmic agent.
• the compounds of formula I, the acid-addition salts or quaternary ammonium derivatives thereof can be transformed into especially cardiac circulation regulating and/or improving, central nervous system tranquillizing and digestive system irregulations improving pharmaceutical formulations in a manner known per se by using pharmaceutically acceptable carriers and/or diluents and/or excipients.
• One dose of the pharmaceutical composition may comprise 0.5 to 500 mg of compounds of formula I, the acid-addition salts or the quaternary ammonium derivatives thereof.
• the invention is further illustrated by the following, non-limiting examples. (The melting points and boiling points appearing in the examples are not corrected.)
• the solvent is distilled off and the product is purified by precipitation from acidic to alkaline medium.
• Example 1/b The process of Example 1/b is followed except that 2-amino-2-methyl propane (8.05 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 1 The process of Example 1 is followed except that instead of 1-chloro-2,3-epoxypropane 1-bromo-2,3-epoxypropane (15.07 g; 0.11 mole) and instead of diisopropyl amine n-hexylamine (11.13 g; 0.11 mole) are used.
• Example 1 The process of Example 1 is followed except that instead of ethanol methanol, and instead of diisopropyl amine 1-methyl-piperazine (11.0 g; 0.11 mole) are used.
• Example 1/b The process of Example 1/b is followed except that 1-phenyl-piperazine (17.85 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 1/b The process of Example 1/b is followed except that 1-phenylmethyl-piperazine (19.39 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 1 The process of Example 1 is followed except that 3,4-dimethoxyphenyl-ethylamine (19.94 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 1 The process of Example 1 is followed except that pyrrolidine (7.82 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 1 The process of Example 1 is followed except that piperidine (9.37 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 1 The process of Example 1 is followed except that hexahydro-1H-azepine (10.91 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 1 The process of Example 1 is followed except that 3-dimethylamino-1-propylamine (11.24 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 1 The process of Example 1 is followed except that 1-(4-chlorophenyl)-piperazine (21.63 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 1 The process of Example 1 is followed except that 2-(2-hydroxyethyl)-piperazine (14.32 g 0.11 mole) is used instead of diisopropyl amine.
• Example 1/b The process of Example 1/b is followed except that morpholine (9.58 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 14 The process of Example 14 is followed except that 1,1-dimethylpropin-2-yl-amine (9.14 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 14 The process of Example 14 is followed except that 1-methyl piperazine (11.0 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 1/a The process of Example 1/a is followed except that toluene is used instead of benzene and 2-(E)-phenylmethylene-cyclooctane-1-one-(E)-oxime (22.93 g; 0.1 mole) is used as oxime.
• Example 18/a The process of Example 18/a is followed.
• Example 18 The process of Example 18 is followed except that 1-methyl-piperazine (11.0 g; 0.11 mole) is used instead of morpholine.
• Example 21 The process of Example 21 is followed except that 2-amino-2-methyl-propane (8.05 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 1/a The process of Example 1/a is followed except that 2-(E)-(2-chlorophenyl-methylene)-cyclohexan-1-one-(E)-oxime (23.57 g; 0.1 mole) is used instead of 2-(E)-phenylmethylene-cyclohexan-1-one-(E)-oxime.
• Example 23/a The process of Example 23/a is followed except that 2-(E)-(2-chlorophenyl-methylene)-cyclohexan-1-one-(E)-oxime is used instead of 2-(E)-(2-chlorophenyl-methylene)-cyclohexan-1-one-(E)-oxime.
• Example 1/b The process of Example 1/b is followed except that 1-amino-2-methyl-propane (8.05 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 25/a The process of Example 25/a is followed.
• Example 1/b The process of Example 1/b is followed except that 2-aminopropanol (6.5 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 1/b The process of Example 1/b is followed except that cyclopropyl amine (6.28 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 27/a The process of Example 27/a is followed.
• Example 1/b The process of Example 1/b is followed except that n-butylamine (8.05 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 27/a The process of Example 27/a is followed.
• Example 1/a The process of Example 1/a is followed except that 2-(E)-(3,4-Dichlorophenyl-methylene)-cyclohexan-1-one-(E)-oxime (27.02 g; 0.1 mole) is used instead of 2-(E)-phenylmethylene-cyclohexan-1-one-(E)-oxime.
• Example 1/b The process of Example 1/b is followed except that dipropyl amine (11.13 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 1/a The process of Example 1/a is followed except that 2-(E)-(2,6-diChlorophenyl-methylene)-cyclohexan-1-one-(E)-oxime (27.02 g; 0.1 mole) is used instead of 2-(E)-phenylmethylene-cyclohexan-1-one-(E)-oxime.
• Example 1/b The process of Example 1/b is followed except that n-propyl amine (6.5 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 35 The process of Example 35 is followed except that 1-methyl-piperazine (11.0 g; 0.11 mole) is used instead of n-propyl amine.
• Example 1/a The process of Example 1/a is followed except that 2-(E)-(2-methoxyphenyl-methylene)-cyclohexan-1-one-(E)-oxime (23.13 g; 0.1 mole) is used instead of 2-(E)-phenylmethylene-cyclohexan-1-one-(E)-oxime.
• Example 37/a The process of Example 37/a is followed.
• Example 1/b The process of Example 1/b is followed except that 1-(2-methoxyphenyl)-piperazine (21.15 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 37/a The process of Example 37/a is followed except that 2-(E)-(3-methoxyphenyl-methylene)-cyclohexan-1-one-(E)-oxime is used instead of 2-(E)-(2-methoxyphenyl-methylene)-cyclohexan-1-one-(E)-oxime.
• Example 37/a The process of Example 37/a is followed except that 2-(E)-(4-methoxyphenyl-methylene)-cyclohexan-1-one-(E)-oxime is used instead of 2-(E)-(2-methoxyphenyl-methylene)-cyclohexan-1-one-(E)-oxime.
• Example 40 The process of Example 40 is followed except that 3-dimethylamino-1-propylamine (11.24 g; 0.11 mole) is used instead of cyclopropyl amine.
• Example 1/a The process of Example 1/a is followed except that 2-(E)-(4-methoxyphenyl-methylene)-cycloheptan-1-one-(E)-oxime (24.53 g; 0.1 mole) is used instead of 2-(E)-phenylmethylene-cyclohexan-1-one-(E)-oxime.
• Example 42/a The process of Example 42/a is followed.
• Example 42/a The process of Example 42/a is followed.
• Example 1/b The process of Example 1/b is followed except that diethyl amine (8.05 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 27/a The process of Example 27/a is followed.
• Example 27/b The process of Example 27/b is followed except that N-methyl-N-cyclohexyl amine (12.45 g; 0.11 mole) is used instead of cyclopropyl amine.
• Example 27/a The process of Example 27/a is followed.
• Example 1/b The process of Example 1/b is followed except that n-propyl amine (6.28 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 1/a The process of Example 1/a is followed except that 2-(E)-(4-chlorophenyl-methyl)-cyclohexan-1-one-(E)-oxime (23.77 g; 0.1 mole) is used instead of 2-(E)-phenylmethylene-cyclohexan-1-one-(E)-oxime.
• Example 18/a The process of Example 18/a is followed.
• Example 18/a The process of Example 18/a is followed.
• Example 42/a The process of Example 42/a is followed.
• Example 42/a The process of Example 42/a is followed.
• Example 1 The process of Example 1 is followed except that 1-(3-chlorophenyl)-piperazine (21.63 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 1 The process of Example 1 is followed except that 1-(3-trifluoromethyl)-phenyl piperazine (25.3 g; 0.11 mole) is used instead of diisopropyl amine.
• Example 1 The process of Example 1 is followed except that 1-phenylmethyl piperidine (19.3 g g; 0.11 mole) is used instead of diisopropyl amine.
• Example 1 The process of Example 1 is followed except that 4-phenyl-1,2,3,6-tetrahydropyridine (17.5 g; 0.11 mole) is used instead of diisopropyl amine. Yield: 32.4 g (77.0%).
• Tablet comprising 25 mg of active ingredient Composition of one tablet is as follows:
• the tablet is prepared as follows:
• the active ingredient and the corn starch are admixed, then wetted with 10-15% by weight of aqueous polyvinylpyrrolidone solution and the mixture is granulated then dried at a temperature of 40° to 50° C.
• the dry granules is rubbed through a sieve, mixed with talcum and magnesium stearate and tablets are prepared from the mixture.
• the weight of one tablet is 300.0 mg.
• Tablet comprising 250 mg of active ingredient
• the composition of one tablet is as follows:
• the active ingredient, lactose and corn starch are wetted and mixed, granulated and dried at a temperature of 40° to 50° C.
• the dry granules are rubbed trough a sieve as described hereinabove, mixed with magnesium stearate and talcum, then tablets are formed.
• the weight of one tablet is 600.0 mg.
• Dragee comprising 25 mg of active ingredient
• the composition of one dragee core is as follows:
• the active ingredient and corn starch are mixed, wetted with 10% by weight aqueous gelatine solution, granules are formed from the wet mixture, then the granules are dried at a temperature of 40° to 50° C. The dry granules are rubbed through a sieve, homogenized with talcum and magnesium stearate and dragee cores of 300.0 mg are compressed from the mixture.
• Dragee comprising 50.0 mg of active ingredient
• the composition of one dragee core is as follows:
• the granules are prepared as described hereinabove.
• the weight of the dragee cores is 150.0 mg.
• the dragee cores are coated with a layer containing sugar and talcum in a manner known per se.
• the dragee thus obtained is painted with non-toxic food paint to the desired colour and polished with bee-wax.
• Gelatine capsule comprising 5.0 mg of active ingredient
• the composition of one gelatine capsule is as follows:
• the ingredients are homogenized and filled into gelatine capsules of suitable size.
• Gelatine capsule comprising 25.0 mg of active ingredient
• the composition of one gelatine capsule is as follows:
• the ingredients are homogenized and filled into gelatine capsules of suitable size.
• Gelatine capsule comprising 50.0 mg of active ingredient
• the composition of one gelatine capsule is as follows:
• the ingredients are homogenized and filled into gelatine capssules of suitable size.
• Gelatine capsule comprising 250.0 mg of active ingredient
• the composition of one gelatine capsule is as follows:
• the ingredients are homogenized and filled into gelatine capsules of suitable size.
• Injection comprising 25.0 mg of active ingredient
• composition of one ampoule is as follows:
• the active ingredient and sodium chloride are dissolved in the necessary amount of twice-distilled water suitable for making injections.
• the solution is filtered, filled into ampoules and sterilized.
• Injection comprising 50.0 mg of active ingredient
• the composition of one ampoule is as follows:
• the active ingredient and sodium chloride are dissolved in the necessary amount of twice-distilled water, then filled into ampoules under sterile conditions.
• Suppository comprising 250 mg of active ingredient
• the composition of one suppository is as follows:
• the fatty acid glyceride is melted, the active ingredient is homogenized, then poured into a mould.
• the sorbitol, the active ingredient, citric acid and sodium citrate are dissolved in the aqueous solution of propylene glycol, then after dissolution of the solid materials, the flavourant is added.
• the solution is filtered off and filled into flasks supplied with a drop-dispenser.
• the base is transformed into (E)-2-butenedioate salt.
• Example 1 The process of Example 1 is followed except that 2-(E)-[3',4'-(methylenedioxide)-phenylmethylene]-cyclohexane-1-one-(E)-oxime (24.5 g; 0.1 mole) is used instead of 2-(E)-phenylmethylene-cyclohexane-1-one-(E)-oxime.
• Example 72/a The process of Example 72/a is followed.
• the mother liquor obtained in the course of the filtration of the (+)-dibenzoyl tartarate salt is evaporated and the (-)-2-(E)-phenylmethylene-1-(E)- ⁇ 3-[bis-(1-methylethyl)-amino]-2-hydroxy-propoxyimino ⁇ -cyclohexane is liberated as described hereinabove from the (-)-2-(E)-phenylmethylene-1-(E)- ⁇ 3-[bis-(1-methylethyl)-amino]-2-hydroxy-propoxyimino ⁇ -cyclohexane-(+)-dibenzoyl tartarate thus obtained.
• the racemic product prepared according to Example 1/b (71.7 g; 0.2 mole) is dissolved in dichloro ethane (200 ml), then water (200 ml) and (-)-dibenzoyl tartaric acid (35.8 g; 0.1 mole) are added.
• the reaction mixture is stirred at a temperature of 15° to 20° C. for 10 hours, and the product is filtered off.
• the dichloro ethane mother liquor obtained during the filtration of the (-)-dibenzoyl tartaric acid salt is evaporated after drying over anhydrous magnesium sulfate.

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• 1989
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• 1991
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